WO2013018416A1 - 室温湿気増粘型熱伝導性シリコーングリース組成物 - Google Patents
室温湿気増粘型熱伝導性シリコーングリース組成物 Download PDFInfo
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- WO2013018416A1 WO2013018416A1 PCT/JP2012/062615 JP2012062615W WO2013018416A1 WO 2013018416 A1 WO2013018416 A1 WO 2013018416A1 JP 2012062615 W JP2012062615 W JP 2012062615W WO 2013018416 A1 WO2013018416 A1 WO 2013018416A1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/50—Lubricating compositions characterised by the base-material being a macromolecular compound containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/16—Polysiloxanes containing silicon bound to oxygen-containing groups to hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
Definitions
- the present invention relates to a room temperature moisture thickening type heat conductive silicone grease composition which is not only easy to apply but also has a very high shape maintaining property and thus has a very good workability.
- Patent Documents 1 to 5 Since it adheres completely in any case, there is a drawback of poor reworkability. In addition, after bonding, the heat conductive material becomes very hard, so the heat conductive material cannot withstand due to repeated stress due to thermal strain, etc. There was a problem that stress was applied to electronic elements and components later.
- the low-viscosity, easy-to-apply initial coating makes it difficult to sag by increasing the room temperature moisture after application, and the dealcohol-free room temperature moisture thickening type thermal conductive silicone grease that can be stored at room temperature.
- a composition was developed. Note that this room temperature moisture thickening type thermally conductive silicone grease composition is not cured with moisture, but is only thickened, so it has excellent reworkability and gives a great stress to the electric element. There is nothing. However, since it has recently been found that long-term durability is poor, particularly at high temperatures, a new room temperature moisture thickened thermally conductive silicone grease composition has been developed to improve this point.
- this room temperature moisture thickening type thermally conductive silicone grease composition has a low viscosity in the initial stage (before thickening), and therefore has poor shape maintenance, and sags (deforms) immediately after application. The problem of work was left.
- the present invention has been made in view of the above circumstances, and has room temperature moisture thickening type heat conduction that has high shape maintainability and excellent workability even at low viscosity (easy to apply) in the initial stage (before thickening).
- An object of the present invention is to provide a functional silicone grease composition.
- Siloxane (B) an organopolysiloxane represented by the following general formula (1), (C) a silane compound having three or more hydrolyzable groups bonded to a silicon atom in one molecule and / or its (part) Hydrolyzate or (partial) hydrolysis condensate, (D) thickening catalyst, (E) thermally conductive filler having a thermal conductivity of 10 W / m ⁇ ° C.
- the room temperature moisture thickening type thermally conductive silicone grease composition is found to have high shape maintenance and excellent workability even in the initial stage (before thickening), even when the viscosity is low (easy to apply). It came to make.
- the present invention provides the room temperature moisture thickened thermally conductive silicone grease composition shown below.
- A Organopolysiloxane having a viscosity of 0.1 to 1,000 Pa ⁇ s at 25 ° C. and having both ends blocked with hydroxyl groups: 5 to 80 parts by mass
- B The following general formula (1) (Wherein R 1 is independently an unsubstituted or substituted monovalent hydrocarbon group, R 2 is independently an alkyl group, an alkoxyalkyl group, an alkenyl group or an acyl group, and n is an integer of 2 to 100) And a is an integer of 1 to 3.) An organopolysiloxane represented by: 20 to 95 parts by mass, (However, the sum of component (A) and component (B) is 100 parts by mass.)
- C a silane compound having three or more hydrolyzable groups bonded to a silicon atom in one molecule and / or its (partial) hydrolyzate or (partial) hydrolysis
- (F) Silica fine powder A room temperature moisture thickening type thermally conductive silicone grease composition comprising 10 to 100 parts by mass of 100 parts by mass of component (A) as an essential component.
- (G) the organosilane represented by the following general formula (2) and / or a partial hydrolysis condensate thereof is contained in an amount of 0.1 to 20 parts by mass with respect to 100 parts by mass in total of the components (A) and (B).
- the room temperature moisture thickened heat conductive silicone grease composition according to [1].
- R 3 b R 4 c Si (OR 5 ) 4-bc (2) (Wherein R 3 is independently an unsubstituted or substituted alkyl group having 6 to 20 carbon atoms, R 4 is independently an unsubstituted or substituted monovalent hydrocarbon group having 1 to 20 carbon atoms; 5 is independently an alkyl group having 1 to 6 carbon atoms, b is an integer of 1 to 3, c is an integer of 0 to 2, and b + c is an integer of 1 to 3.) [3] Further, (H) an organopolysiloxane having a viscosity at 25 ° C.
- composition formula (3) of 0.05 to 1,000 Pa ⁇ s is based on a total of 100 parts by mass of the components (A) and (B).
- R 6 is independently an unsubstituted or substituted monovalent hydrocarbon group having 1 to 18 carbon atoms, and d is a positive number of 1.8 ⁇ d ⁇ 2.2.
- Hydrolyzable having a group selected from the group consisting of an amino group, an epoxy group, a mercapto group, an acryloyl group and a methacryloyl group bonded to a silicon atom via a carbon atom and bonded to a silicon atom [1], [2] or [3] containing 0.01 to 30 parts by mass of the silane compound having a group and / or a partial hydrolysis-condensation product thereof with respect to 100 parts by mass in total of the components (A) and (B) The room temperature moisture thickened heat conductive silicone grease composition as described.
- the room temperature moisture thickened heat conductive silicone grease composition of the present invention is not only easy to apply in the initial stage (before thickening), but also has a very high shape maintainability, so that workability is very good. Unlike adhesive materials, potting materials, and room temperature-curing thermal conductive silicone rubber compositions, it only thickens without curing, so it has excellent repairability even after thickening, and it may cause great stress on electronic devices. Nor.
- the initial (before thickening) has a low viscosity and can be freely deformed according to the unevenness, so that even if the heat generating part has a complicated shape, it can be adhered to every corner.
- Component (A) is a base polymer (main agent) of the present composition and is an organopolysiloxane having both ends blocked with hydroxyl groups.
- Other structures are not particularly limited as long as they have hydroxyl groups at both ends, and may be any material that cures and gives an elastomer, such as a normal linear organopolysiloxane, and bonds to a silicon atom.
- substituents examples include an alkyl group such as a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group and a heptyl group, a cycloalkyl group such as a cyclohexyl group, an alkenyl group such as a vinyl group and an allyl group, and a phenyl group
- a monovalent hydrocarbon group having 1 to 8 carbon atoms, preferably 1 to 7 carbon atoms such as an aryl group such as a tolyl group, or a part or all of the hydrogen atoms of these monovalent hydrocarbon groups is a chlorine atom or a fluorine atom
- halogenated hydrocarbon groups such as a chloromethyl group, a 3-chloropropyl group and a trifluoromethyl group substituted with a halogen atom such as a bromine atom.
- the viscosity of component (A) at 25 ° C. is 0.1 to 1,000 Pa ⁇ s, preferably 0.3 to 100 Pa ⁇ s, and more preferably 0.5 to 50 Pa ⁇ s.
- the viscosity is lower than 0.1 Pa ⁇ s, the thickening is delayed, and when it is higher than 1,000 Pa ⁇ s, the room temperature moisture thickening type thermally conductive silicone grease composition has a high viscosity. Will get worse.
- This viscosity is a value measured with a rotational viscometer (hereinafter the same).
- an organopolysiloxane represented by the following general formula (4) is more preferably used as the component (A).
- R 7 is an unsubstituted or substituted monovalent hydrocarbon group having 1 to 8 carbon atoms, preferably 1 to 7 carbon atoms, which is the same or different from each other, and specifically includes a methyl group, an ethyl group, Monovalent hydrocarbon groups such as alkyl groups such as propyl group, butyl group, pentyl group, hexyl group and heptyl group, aryl groups such as phenyl group and tolyl group, and part or all of hydrogen atoms of these monovalent hydrocarbon groups Is a halogen-substituted hydrocarbon group such as a chloromethyl group, a 3-chloropropyl group, a trifluoromethyl group or a cyanoethyl group substituted with a halogen atom such as a chlorine atom, a fluorine atom or a bromine atom, or a cyano group, or a cyano group-substituted carbon
- m is a number that makes the viscosity of the organopolysiloxane represented by the formula (4) at 25 ° C. 0.1 to 1,000 Pa ⁇ s, preferably 0.3 to 100 Pa ⁇ s.
- a component may be used individually by 1 type, or may use 2 or more types together.
- the component (A) is not thickened when the amount is less than 5 parts by mass in 100 parts by mass of the component (A) and the component (B). Since a product cannot be obtained, it is used in the range of 5 to 80 parts by mass, preferably in the range of 10 to 70 parts by mass.
- the component (B) used in the present invention is an organopolysiloxane represented by the following general formula (1), preferably having a viscosity at 25 ° C. of 0.005 to 100 Pa ⁇ s.
- the component (B) plays an important role of keeping the composition in a grease state even after thickening without hardening the composition.
- R 1 is independently an unsubstituted or substituted monovalent hydrocarbon group
- R 2 is independently an alkyl group, an alkoxyalkyl group, an alkenyl group or an acyl group
- n is an integer of 2 to 100
- a is an integer of 1 to 3.
- R 1 is independently an unsubstituted or substituted monovalent hydrocarbon group having preferably 1 to 10 carbon atoms, more preferably 1 to 6 carbon atoms, still more preferably 1 to 3 carbon atoms.
- Examples thereof include a linear alkyl group, a branched alkyl group, a cyclic alkyl group, an alkenyl group, an aryl group, an aralkyl group, a halogenated alkyl group, and a cyanoalkyl group.
- Examples of the linear alkyl group include a methyl group, an ethyl group, a propyl group, a hexyl group, and an octyl group.
- Examples of the branched alkyl group include isopropyl group, isobutyl group, tert-butyl group, and 2-ethylhexyl group.
- Examples of the cyclic alkyl group include a cyclopentyl group and a cyclohexyl group.
- Examples of the alkenyl group include a vinyl group and an allyl group.
- Examples of the aryl group include a phenyl group and a tolyl group.
- Examples of the aralkyl group include a 2-phenylethyl group and a 2-methyl-2-phenylethyl group.
- halogenated alkyl group examples include a 3,3,3-trifluoropropyl group, a 2- (nonafluorobutyl) ethyl group, and a 2- (heptadecafluorooctyl) ethyl group.
- cyanoalkyl group examples include a cyanoethyl group.
- R 1 is preferably a methyl group, a phenyl group, or a vinyl group.
- R 2 is independently an alkyl group, an alkoxyalkyl group, an alkenyl group, or an acyl group.
- alkyl group include linear alkyl groups, branched alkyl groups, and cyclic alkyl groups similar to those exemplified for R 1 .
- alkoxyalkyl group include a methoxyethyl group and a methoxypropyl group.
- acyl group include an acetyl group and an octanoyl group.
- R 2 is preferably an alkyl group, particularly preferably a methyl group or an ethyl group.
- N is an integer of 2 to 100, preferably 5 to 80.
- a is an integer of 1 to 3, preferably 3.
- the viscosity of component (B) at 25 ° C. is usually 0.005 to 100 Pa ⁇ s, particularly preferably 0.005 to 50 Pa ⁇ s. If the viscosity is lower than 0.005 Pa ⁇ s, oil bleed is likely to occur from the room temperature moisture thickened heat conductive silicone grease composition obtained, and there is a possibility that it will easily sag. When the viscosity is higher than 100 Pa ⁇ s, the fluidity of the resulting room temperature moisture thickened heat conductive silicone grease composition becomes poor, and the coating workability may be deteriorated.
- suitable component (B) include the following. (In the formula, Me is a methyl group.) (B) A component may be used individually by 1 type, or may use 2 or more types together.
- the component (B) is less than 20 parts by mass in a total of 100 parts by mass of the component (A) and the component (B), it becomes hard after thickening and a soft composition cannot be obtained. If the amount is too large, the viscosity does not increase, so the amount is used in the range of 20 to 95 parts by weight, and more preferably in the range of 30 to 90 parts by weight.
- Component (C) is a silane compound having three or more hydrolyzable groups bonded to a silicon atom in one molecule, its (partial) hydrolyzate or (partial) hydrolysis condensate, and the composition of the present invention. Acts as a thickener.
- silane compound those represented by the following general formula (5) are preferably used.
- R 8 is an unsubstituted or substituted monovalent hydrocarbon group having preferably 1 to 10 carbon atoms, more preferably 1 to 6 carbon atoms.
- R 1 in the above formula (1) or the formula (4 ) The same groups as R 7 are exemplified, but an alkyl group having 1 to 3 carbon atoms, a vinyl group, and a phenyl group are particularly preferable.
- X is a hydrolyzable group, and examples thereof include an alkoxy group, an alkoxyalkoxy group, an alkenyloxy group, a ketoxime group, an acyloxy group, an amino group, an amide group, and an aminoxy group.
- the alkoxy group and alkoxyalkoxy group may be substituted with a halogen atom.
- a halogen atom For example, methoxy group, ethoxy group, isopropoxy group, butoxy group, ⁇ -chloroethoxy group, 2,2,2-trifluoroethoxy Group, ⁇ -chlorobutoxy group, methoxyethoxy group and the like.
- alkenyloxy group include an isopropenoxy group.
- Examples of the ketoxime group include a dimethyl ketoxime group, a methyl ethyl ketoxime group, and a diethyl ketoxime group.
- the acyloxy group include an acetoxy group and a propionyloxy group.
- Examples of the amino group include a dimethylamino group, a diethylamino group, an n-butylamino group, and a cyclohexylamino group.
- Examples of the amide group include an N-methylacetamide group, an N-ethylacetamide group, an N-butylacetamide group, an N-cyclohexylacetamide group, and the like.
- Examples of the aminoxy group include N, N-dimethylaminoxy group, N, N-diethylaminoxy group and the like.
- X is particularly preferably an alkenyloxy group.
- e is 0 or 1.
- silane compounds their (partial) hydrolysates or (partial) hydrolysis condensates include tetramethoxysilane, tetraethoxysilane, methyltrimethoxysilane, ethyltrimethoxysilane, vinyltrimethoxysilane, 3, 3,3-trifluoropropyltrimethoxysilane, ⁇ -cyanoethyltrimethoxysilane, tetraisopropoxysilane, tetrabutoxysilane, phenyltrimethoxysilane, octadecyltrimethoxysilane, tetra ( ⁇ -chloroethoxy) silane, tetra (2, 2,2-trifluoroethoxy) silane, propyltris ( ⁇ -chlorobutoxy) silane, alkoxysilanes such as methyltris (methoxyethoxy) silane, ethylpolys
- ketoximesilanes methyltris (cyclohexyl) Aminosilanes such as amino) silane, vinyltris (n-butylamino) silane, amidesilanes such as methyltris (N-methylacetamido) silane, methyltris (N-butylacetamido) silane, methyltris (N-cyclohexylacetamido) silane, methyltris ( Aminoxysilanes such as N, N-diethylaminoxy) silane, methyltri (isopropenoxy) silane, vinyltri (iso Ropenokishi) silane, alkenyloxy silane such as phenyl tri (isopropenoxy) silane, methyltriacetoxysilane, and the like acyloxy such as vinyltriacetoxysilane.
- a component may be used individually by 1 type, or may use 2 or more types together.
- the blending amount of the component (C) does not increase when the amount is less than 1 part by mass with respect to a total of 100 parts by mass of the component (A) and the component (B), and increases even when the amount exceeds 30 parts by mass. Since it is difficult, it is in the range of 1 to 30 parts by mass, preferably in the range of 1 to 20 parts by mass.
- the room temperature moisture thickening type thermally conductive silicone grease composition of the present invention is a condensation thickening type, and in this composition, a thickening catalyst (condensation catalyst) is used as component (D).
- a thickening catalyst condensation catalyst
- silane or siloxane containing a guanidyl group such as tetramethylguanidylpropyltrimethoxysilane, tetramethylguanidylpropylmethyldimethoxysilane, tetramethylguanidylpropyltris (trimethylsiloxy) silane, or the like is preferably used. .
- component (D) added When the amount of component (D) added is less than 0.01 parts by weight relative to a total of 100 parts by weight of component (A) and component (B), it will be difficult to thicken and the amount will exceed 20 parts by weight. Since it is uneconomical, it is in the range of 0.01 to 20 parts by mass, preferably in the range of 0.1 to 5 parts by mass.
- the heat conductive filler having the thermal conductivity of the component (E) if the heat conductivity of the filler is less than 10 W / m ⁇ ° C., the heat of the room temperature moisture thickened type heat conductive silicone grease composition Since the conductivity itself is small, a filler having a thermal conductivity of 10 W / m ⁇ ° C. or higher, preferably 15 W / m ⁇ ° C. or higher is used.
- Such heat conductive fillers include aluminum powder, copper powder, silver powder, nickel powder, gold powder, alumina powder, zinc oxide powder, magnesium oxide powder, aluminum nitride powder, boron nitride powder, silicon nitride powder, diamond Examples thereof include powder and carbon powder, but any filler may be used as long as the thermal conductivity is 10 W / m ⁇ ° C. or more, and one kind or two or more kinds may be mixed.
- the average particle size of the thermally conductive filler is less than 0.1 ⁇ m, it may not be in the form of a grease and may have poor extensibility. If it is greater than 300 ⁇ m, the room temperature moisture thickened type thermally conductive silicone grease composition Since the uniformity may be poor, the range of 0.1 to 300 ⁇ m is preferable, and the range of 0.1 to 200 ⁇ m is more preferable.
- the shape of the filler may be indefinite, spherical or any shape.
- an average particle diameter can be calculated
- the amount of the heat conductive filler is less than 100 parts by mass with respect to the total of 100 parts by mass of the component (A) and the component (B), the desired thermal conductivity cannot be obtained, and it is more than 2,000 parts by mass. Therefore, it is in the range of 100 to 2,000 parts by mass, and preferably in the range of 200 to 1,500 parts by mass.
- Component silica fine powder is a component that imparts shape maintenance to the composition.
- silica fine powder surface-treated fumed silica is preferably used. By performing the surface treatment, dispersibility is improved with respect to the component (A) and the component (B), and uniform dispersion becomes possible. Moreover, shape maintenance property can be given by the interaction between surface-treated fumed silica and between the surface-treated fumed silica and the components (A), (B), and (C).
- chlorosilane, silazane, siloxane and the like are effective.
- Specific examples of the surface treatment agent include methyltrichlorosilane, dimethyldichlorosilane, trimethylchlorosilane, hexamethyldisilazane, octamethylcyclotetrasiloxane, ⁇ , ⁇ -trimethylsilyldimethylpolysiloxane, and the like.
- the specific surface area (BET method) of the component (F) is preferably 50 m 2 / g or more, and particularly preferably 100 m 2 / g or more. If it is less than 50 m 2 / g, the initial viscosity of the room temperature moisture thickened heat conductive silicone grease composition becomes too high, and workability may deteriorate.
- the specific surface area (BET method) is preferably 500 m 2 / g or less, particularly 300 m 2 / g or less because the shape maintaining performance is improved.
- the amount of the component (F) is less than 10 parts by mass relative to 100 parts by mass of the component (A), the shape cannot be maintained, and when it exceeds 100 parts by mass, it does not become a grease and has poor extensibility. Therefore, it is in the range of 10 to 100 parts by mass, preferably in the range of 10 to 50 parts by mass, and more preferably in the range of 10.1 to 45 parts by mass.
- the room temperature moisture thickened thermally conductive silicone grease composition of the present invention may further contain (G) an organosilane represented by the following general formula (2) and / or a partial hydrolysis condensate thereof.
- R 3 b R 4 c Si (OR 5 ) 4-bc (2) (Wherein R 3 is independently an unsubstituted or substituted alkyl group having 6 to 20 carbon atoms, R 4 is independently an unsubstituted or substituted monovalent hydrocarbon group having 1 to 20 carbon atoms; 5 is independently an alkyl group having 1 to 6 carbon atoms, b is an integer of 1 to 3, c is an integer of 0 to 2, and b + c is an integer of 1 to 3.)
- R 3 is independently an unsubstituted or substituted alkyl group having 6 to 20 carbon atoms.
- groups include hexyl groups, octyl groups, decyl groups, dodecyl groups, tetradecyl groups, hexadecyl groups, octadecyl groups and other alkyl groups, and some or all of the hydrogen atoms of these groups are chlorine atoms, fluorine Examples thereof include halogenated alkyl groups such as 2- (perfluorobutyl) ethyl group and 2- (perfluorooctyl) ethyl group substituted with halogen atoms such as atoms and bromine atoms. An alkyl group is preferred.
- R 4 is independently an unsubstituted or substituted monovalent hydrocarbon group having 1 to 20 carbon atoms, preferably 1 to 10 carbon atoms.
- groups include, for example, methyl groups, ethyl groups, propyl groups, hexyl groups, octyl groups, decyl groups, alkyl groups such as dodecyl groups, tetradecyl groups, hexadecyl groups, octadecyl groups, cyclopentyl groups, cyclohexyl groups, etc.
- Alkyl groups such as cycloalkyl groups, vinyl groups and allyl groups; aryl groups such as phenyl groups and tolyl groups; aralkyl groups such as 2-phenylethyl groups and 2-methyl-2-phenylethyl groups; and hydrogen atoms of these groups 3,3,3-trifluoropropyl group, 2- (perfluorobutyl) ethyl group, 2- (perfluorooctyl) in which a part or all of is substituted with a halogen atom such as a chlorine atom, a fluorine atom or a bromine atom Examples thereof include halogenated hydrocarbon groups such as an ethyl group and a p-chlorophenyl group, and a methyl group is particularly preferable.
- R 5 is one or more alkyl groups having 1 to 6 carbon atoms such as a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group and a hexyl group, and a methyl group and an ethyl group are particularly preferable.
- b is an integer of 1 to 3
- c is an integer of 0 to 2.
- b + c is 1, 2 or 3, and 1 is particularly preferable.
- C 10 H 21 Si (OCH 3 ) 3 C 10 H 21 Si (OCH 2 CH 3 ) 3 , C 14 H 29 Si (OCH 3 ) 3 , C 14 H 29 Si (OCH 2 CH 3 ) 3 Etc.
- a component may be used individually by 1 type, or may use 2 or more types together.
- the amount of addition of the organosilane of component (G) and / or its partial hydrolysis condensate is less than 0.1 parts by mass relative to a total of 100 parts by mass of component (A) and component (B)
- the effect of lowering the viscosity of the composition may be reduced, and the effect is not increased even if the amount is more than 20 parts by mass, which is uneconomical. Therefore, the range of 0.1 to 20 parts by mass is preferable, More preferably, it is in the range of 0.2 to 15 parts by mass.
- the room temperature moisture thickened thermally conductive silicone grease composition of the present invention further comprises (H) a molecular chain having a viscosity at 25 ° C. of 0.05 to 1,000 Pa ⁇ s, represented by the following average composition formula (3):
- a linear organopolysiloxane having a terminal end blocked with a triorganosiloxy group, particularly a trialkylsiloxy group, can be preferably blended, and this can give an effect of adjusting the initial viscosity.
- R 6 d SiO (4-d) / 2 (3) (In the formula, R 6 is independently an unsubstituted or substituted monovalent hydrocarbon group having 1 to 18 carbon atoms, and d is a positive number of 1.8 ⁇ d ⁇ 2.2.)
- R 6 is an unsubstituted or substituted monovalent hydrocarbon group having 1 to 18 carbon atoms.
- groups include alkyl groups such as methyl group, ethyl group, propyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, dodecyl group, tetradecyl group, hexadecyl group, and octadecyl group.
- cycloalkyl group such as cyclopentyl group, cyclohexyl group, alkenyl group such as vinyl group, allyl group, aryl group such as phenyl group, tolyl group, 2-phenylethyl group, 2-methyl-2-phenylethyl group, etc.
- Aralkyl groups 3,3,3-trifluoropropyl groups in which some or all of the hydrogen atoms in these groups are substituted with halogen atoms such as chlorine atoms, fluorine atoms, bromine atoms, etc., 2- (perfluorobutyl) ethyl Groups, halogenated hydrocarbon groups such as 2- (perfluorooctyl) ethyl group, p-chlorophenyl group, etc. That, but in particular a methyl group, a phenyl group, and an alkyl group having 6 to 14 carbon atoms preferred.
- d is preferably a positive number in the range of 1.8 to 2.2, particularly in the range of 1.9 to 2.2, from the viewpoint of the viscosity required for the room temperature moisture thickened heat conductive silicone grease composition. A positive number is preferred.
- the viscosity of the organopolysiloxane at 25 ° C. is lower than 0.05 Pa ⁇ s, oil bleed may easily occur when the room temperature moisture thickened heat conductive silicone grease composition is obtained, and 1,000 Pa.
- the temperature is higher than s, the applicability of the room temperature moisture thickening type heat conductive silicone grease composition may be poor, so the viscosity at 25 ° C. is preferably 0.05 to 1,000 Pa ⁇ s, particularly It is preferably 0.5 to 100 Pa ⁇ s.
- suitable component (H) include the following. (In the formula, Me is a methyl group.) (H) A component may be used individually by 1 type, or may use 2 or more types together.
- the blending amount when the component (H) is used is less than 10 parts by mass with respect to the total of 100 parts by mass of the component (A) and the component (B). If it is more, the room temperature moisture thickening type thermally conductive silicone grease composition may not easily increase in viscosity due to moisture, so the range of 10 to 1,000 parts by mass is preferable, and 20 to 500 parts by mass is preferable. A range is more preferred.
- the room temperature moisture thickened thermally conductive silicone grease composition of the present invention further comprises (I) a group consisting of an amino group, an epoxy group, a mercapto group, an acryloyl group and a methacryloyl group bonded to a silicon atom via a carbon atom.
- a silane compound having a selected functional group and a hydrolyzable group bonded to a silicon atom and / or a partial hydrolysis condensate thereof can be blended. This component plays the role which improves the adhesiveness of this invention composition and an application
- silane compound and its partially hydrolyzed condensate When two or more of the above functional groups are present in the silane compound and its partially hydrolyzed condensate, they may be bonded to a silicon atom via different carbon atoms, or silicon via the same carbon atom. It may be bonded to an atom.
- the silane compound and its partial hydrolysis condensate preferably have 1 to 3, more preferably 2 to 3 hydrolyzable groups.
- the hydrolyzable group include those similar to the hydrolyzable group X in the formula (5) of the component (C), and among them, an alkoxy group is preferable.
- silane compound examples include 3-aminopropyldimethoxymethylsilane, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3- (2-aminoethylamino) propyldimethoxymethylsilane, 3- ( Amino group-containing silanes such as 2-aminoethylamino) propyltrimethoxysilane, 2-aminoethylaminomethyldimethoxymethylsilane, 2-aminoethylaminomethyltrimethoxysilane, ⁇ -mercaptopropyltrimethoxysilane, ⁇ -mercaptopropyltrimethoxysilane, ⁇ -mercaptopropyl Mercapto group-containing silanes such as triethoxysilane, ⁇ -mercaptopropylmethyldimethoxysilane, ⁇ -mercaptopropylmethyldiethoxysilane, 3-glycidoxypropy
- the blending amount when blending the above component (I) is less than 0.01 parts by weight with respect to the total of 100 parts by weight of the component (A) and the component (B). If the amount is more than 30 parts by mass, an improvement in adhesion is not observed and it is uneconomical. Therefore, the range of 0.01 to 30 parts by mass is preferable, and the range of 0.1 to 20 parts by mass is more preferable.
- additives known as additives for room temperature moisture thickening type heat conductive silicone grease compositions may be added within a range that does not impair the purpose of the present invention.
- the additive include reinforcing properties such as calcium carbonate, non-reinforcing fillers, and polyethers as thixotropy improvers.
- colorants such as a pigment and dye, as needed.
- the room temperature moisture thickened heat conductive silicone grease composition of the present invention can be prepared by uniformly mixing the above components by a known method.
- the obtained room temperature moisture thickened heat conductive silicone grease composition has an initial viscosity at 25 ° C. of preferably 10 to 300 Pa ⁇ s, particularly 50 to 250 Pa ⁇ s.
- the room temperature moisture thickening type heat conductive silicone grease composition of the present invention has a low viscosity at the initial stage (before thickening) and can be freely deformed according to the unevenness, so that the heat generating part has a complicated shape. Even if it exists, it is possible to make it contact
- the room temperature moisture thickening type thermally conductive silicone grease composition of the present invention has a viscosity at 500 ° C. of 500 to 50 ° C. after standing for 23 ⁇ 2 ° C./50 ⁇ 5% RH / 7 days (after thickening by moisture). It is preferably 2,000 Pa ⁇ s, particularly 700 to 1,900 Pa ⁇ s.
- the room temperature moisture thickening type thermally conductive silicone grease composition obtained in this way as described above, only thickens without curing, so that it does not sag when used as a heat-dissipating grease and has a repair property. It is very good and there is no worry of applying large stress to the electronic device. Furthermore, since heat resistance is also favorable, it can be used in a wide range of fields where heat dissipation and heat resistance are required, such as in the fields of electric and electronics and transportation equipment.
- Component A-1 Dimethylpolysiloxane having a viscosity at 25 ° C. of 5 Pa ⁇ s and both ends blocked with hydroxyl groups
- A-2 A viscosity at 25 ° C. of 20 Pa ⁇ s and both ends having hydroxyl groups
- A-3 (for comparison): viscosity at 25 ° C. is 0.08 Pa ⁇ s
- dimethylpolysiloxane A-4 blocked at both ends with hydroxyl groups for comparison: viscosity at 25 ° C. Is 1,100 Pa ⁇ s and both ends are blocked with hydroxyl groups.
- Component F-1 Dry fumed silica having a BET specific surface area of 120 m 2 / g and hydrophobized with dimethyldichlorosilane
- Component (I) The following amino group-containing silane I-1: 3-aminopropyltriethoxysilane
- Examples 1 to 5 and Comparative Examples 1 to 6 The compositions of Examples 1 to 5 and Comparative Examples 1 to 6 were obtained by mixing the components (A) to (I) in the amounts shown in Tables 2 and 3 as follows. That is, in a 5 liter gate mixer (Inoue Seisakusho Co., Ltd., trade name: 5 liter planetary mixer), the components (A), (B), and (E) were taken at the blending amounts shown in Tables 2 and 3, and 150 ° C. And deaerated and mixed for 3 hours. Thereafter, the mixture was cooled to room temperature, components (C), (D) and (F) were added, and the mixture was deaerated and mixed at room temperature to be uniform.
- a 5 liter gate mixer Inoue Seisakusho Co., Ltd., trade name: 5 liter planetary mixer
- the components (A), (B), and (E) were taken at the blending amounts shown in Tables 2 and 3, and 150 ° C. And deaerated and mixed for 3 hours. Thereafter, the
- the initial viscosity of the room temperature moisture thickening type heat conductive silicone grease composition showed a value at 25 ° C., and a Malcolm viscometer (type PC-10AA) was used for the measurement.
- thermal conductivity before thickening of the room temperature moisture thickened thermal conductive silicone grease composition at 23 ° C. was measured using a hot disk method thermophysical property measuring apparatus TPA-501 manufactured by Kyoto Electronics Industry Co., Ltd.
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Abstract
Description
〔1〕
(A)25℃における粘度が0.1~1,000Pa・sであり、両末端が水酸基で封鎖されたオルガノポリシロキサン: 5~80質量部、
(B)下記一般式(1)
で表されるオルガノポリシロキサン: 20~95質量部、
(但し、(A)成分と(B)成分の合計は、100質量部である。)
(C)ケイ素原子に結合した加水分解可能な基を1分子中に3個以上有するシラン化合物及び/又はその(部分)加水分解物もしくは(部分)加水分解縮合物: 1~30質量部、
(D)増粘触媒: 0.01~20質量部、
(E)10W/m・℃以上の熱伝導率を有する熱伝導性充填剤: 100~2,000質量部、
(F)シリカ微粉末: (A)成分100質量部に対して10~100質量部
を必須成分とすることを特徴とする室温湿気増粘型熱伝導性シリコーングリース組成物。
〔2〕
更に、(G)下記一般式(2)で示されるオルガノシラン及び/又はその部分加水分解縮合物を、(A)、(B)成分の合計100質量部に対し0.1~20質量部含む〔1〕記載の室温湿気増粘型熱伝導性シリコーングリース組成物。
R3 bR4 cSi(OR5)4-b-c (2)
(式中、R3は独立に炭素数6~20の非置換又は置換のアルキル基であり、R4は独立に炭素数1~20の非置換又は置換の1価炭化水素基であり、R5は独立に炭素数1~6のアルキル基であり、bは1~3の整数、cは0~2の整数で、b+cは1~3の整数である。)
〔3〕
更に、(H)下記平均組成式(3)で示される25℃における粘度が0.05~1,000Pa・sのオルガノポリシロキサンを、(A)、(B)成分の合計100質量部に対し10~1,000質量部含む〔1〕又は〔2〕記載の室温湿気増粘型熱伝導性シリコーングリース組成物。
R6 dSiO(4-d)/2 (3)
(式中、R6は独立に炭素数1~18の非置換又は置換の1価炭化水素基であり、dは1.8≦d≦2.2の正数である。)
〔4〕
更に、(I)炭素原子を介してケイ素原子に結合したアミノ基、エポキシ基、メルカプト基、アクリロイル基及びメタクリロイル基からなる群から選択される基を有し、且つケイ素原子に結合した加水分解性基を有するシラン化合物及び/又はその部分加水分解縮合物を、(A)、(B)成分の合計100質量部に対し0.01~30質量部含む〔1〕、〔2〕又は〔3〕記載の室温湿気増粘型熱伝導性シリコーングリース組成物。
〔5〕
(F)成分のシリカ微粉末が、表面処理煙霧質シリカである〔1〕~〔4〕のいずれかに記載の室温湿気増粘型熱伝導性シリコーングリース組成物。
〔6〕
(D)成分の増粘触媒が、グアニジル基を含有するシラン又はシロキサンである〔1〕~〔5〕のいずれかに記載の室温湿気増粘型熱伝導性シリコーングリース組成物。
(A)成分は、本組成物のベースポリマー(主剤)であり、両末端が水酸基で封鎖されたオルガノポリシロキサンである。両末端に水酸基を有していれば、それ以外の構造は特に限定されず、通常の直鎖状のオルガノポリシロキサン等の、硬化してエラストマーを与えるものであればよく、ケイ素原子に結合する置換基としては、メチル基、エチル基、プロピル基、ブチル基、ペンチル基、ヘキシル基、ヘプチル基等のアルキル基、シクロヘキシル基等のシクロアルキル基、ビニル基、アリル基等のアルケニル基、フェニル基、トリル基等のアリール基などの炭素数1~8、好ましくは炭素数1~7の1価炭化水素基、あるいはこれら1価炭化水素基の水素原子の一部又は全部を塩素原子、フッ素原子、臭素原子等のハロゲン原子で置換したクロロメチル基、3-クロロプロピル基、トリフルオロメチル基等のハロゲン化炭化水素基などが挙げられる。
mは、式(4)で示されるオルガノポリシロキサンの25℃における粘度を0.1~1,000Pa・s、好ましくは0.3~100Pa・sとする数である。
(A)成分は1種を単独で用いても、2種以上を併用してもよい。
(B)成分は、組成物を硬化させ切らずに増粘後もグリース状に留めておく重要な役割を担っている。
R8 eSiX4-e (5)
Xは加水分解性基であり、アルコキシ基、アルコキシアルコキシ基、アルケニルオキシ基、ケトオキシム基、アシロキシ基、アミノ基、アミド基、アミノキシ基等が例示される。アルコキシ基、アルコキシアルコキシ基としては、ハロゲン原子置換のものであってもよく、例えば、メトキシ基、エトキシ基、イソプロポキシ基、ブトキシ基、β-クロロエトキシ基、2,2,2-トリフルオロエトキシ基、δ-クロロブトキシ基、メトキシエトキシ基等が挙げられる。アルケニルオキシ基としては、例えば、イソプロペノキシ基等が挙げられる。ケトオキシム基としては、例えば、ジメチルケトオキシム基、メチルエチルケトオキシム基、ジエチルケトオキシム基等が挙げられる。アシロキシ基としては、例えば、アセトキシ基、プロピオニルオキシ基等が挙げられる。アミノ基としては、例えば、ジメチルアミノ基、ジエチルアミノ基、n-ブチルアミノ基、シクロヘキシルアミノ基等が挙げられる。アミド基としては、例えば、N-メチルアセトアミド基、N-エチルアセトアミド基、N-ブチルアセトアミド基、N-シクロヘキシルアセトアミド基等が挙げられる。アミノキシ基としては、例えば、N,N-ジメチルアミノキシ基、N,N-ジエチルアミノキシ基等が挙げられる。Xとしては、特にアルケニルオキシ基が好ましい。
eは0又は1である。
(C)成分は1種を単独で用いても、2種以上を併用してもよい。
R3 bR4 cSi(OR5)4-b-c (2)
(式中、R3は独立に炭素数6~20の非置換又は置換のアルキル基であり、R4は独立に炭素数1~20の非置換又は置換の1価炭化水素基であり、R5は独立に炭素数1~6のアルキル基であり、bは1~3の整数、cは0~2の整数で、b+cは1~3の整数である。)
bは1~3の整数、cは0~2の整数である。b+cは1、2又は3であり、特に1であることが好ましい。
C10H21Si(OCH3)3、
C10H21Si(OCH2CH3)3、
C14H29Si(OCH3)3、
C14H29Si(OCH2CH3)3
などが例示できる。
(G)成分は1種を単独で用いても、2種以上を併用してもよい。
R6 dSiO(4-d)/2 (3)
(式中、R6は独立に炭素数1~18の非置換又は置換の1価炭化水素基であり、dは1.8≦d≦2.2の正数である。)
dは、室温湿気増粘型熱伝導性シリコーングリース組成物として要求される粘度の観点から、1.8~2.2の範囲の正数がよく、特に1.9~2.2の範囲の正数が好ましい。
(I)成分は、その1種に限定されず、2種もしくはそれ以上の混合物として使用してもよい。
また、本発明の室温湿気増粘型熱伝導性シリコーングリース組成物は、接着材料や、ポッティング材料、室温硬化型熱伝導性シリコーンゴム組成物とは異なり、硬化することなく増粘することが特徴であり、湿気さえあれば室温でも増粘できるので加熱工程も不要である。また一旦増粘してしまえば、垂直置きにしても垂れ難くなる。更に、本発明の室温湿気増粘型熱伝導性シリコーングリース組成物は、保存時に冷蔵保存や冷凍保存する必要もない。
(A)成分
A-1: 25℃における粘度が5Pa・sであり、両末端が水酸基で封鎖されたジメチルポリシロキサン
A-2: 25℃における粘度が20Pa・sであり、両末端が水酸基で封鎖されたジメチルポリシロキサン
A-3(比較用): 25℃における粘度が0.08Pa・sであり、両末端が水酸基で封鎖されたジメチルポリシロキサン
A-4(比較用): 25℃における粘度が1,100Pa・sであり、両末端が水酸基で封鎖されたジメチルポリシロキサン
C-1: フェニルトリ(イソプロペノキシ)シラン
C-2: ビニルトリ(イソプロペノキシ)シラン
D-1: テトラメチルグアニジルプロピルトリメトキシシラン
5リットルゲートミキサー(井上製作所株式会社製・商品名:5リットルプラネタリミキサー)を用いて、下記に示す熱伝導性充填剤を下記表1に示す混合比で室温にて15分攪拌することによりE-1、E-2を得た。なお、E-3は酸化亜鉛粉末のみである。
平均粒径10μmのアルミナ粉末(熱伝導率:27W/m・℃)
平均粒径15μmのアルミニウム粉末(熱伝導率:236W/m・℃)
平均粒径1.0μmの酸化亜鉛粉末(熱伝導率:25W/m・℃)
F-1: BET比表面積が120m2/gであり、ジメチルジクロロシランにより疎水化処理された乾式ヒュームドシリカ
下記式で表されるオルガノシラン
G-1: C10H21Si(OCH3)3
下記のアミノ基含有シラン
I-1: 3-アミノプロピルトリエトキシシラン
(A)~(I)成分を表2及び表3に示す配合量で以下のように混合して実施例1~5及び比較例1~6の組成物を得た。即ち、5リットルゲートミキサー(井上製作所株式会社製・商品名:5リットルプラネタリミキサー)に、(A)、(B)、(E)成分を表2及び表3に示す配合量で取り、150℃で3時間脱気加熱混合した。その後常温になるまで冷却し、(C)、(D)及び(F)成分を加え、均一になるように室温にて脱気混合した。必要に応じて(G)、(H)あるいは(I)成分を加え、均一になるように室温にて脱気混合した。このようにして得られた組成物について、粘度、熱伝導率及び形状維持特性を下記に示す方法により評価した。その結果を表2及び表3に併記する。
室温湿気増粘型熱伝導性シリコーングリース組成物の初期粘度は25℃における値を示し、その測定はマルコム粘度計(タイプPC-10AA)を用いた。
室温湿気増粘型熱伝導性シリコーングリース組成物を3.0mmのシート状にして、23±2℃/50±5%RHに7日間放置し、その粘度を25℃においてマルコム粘度計(タイプPC-10AA)を用いて測定した。
京都電子工業株式会社製ホットディスク法熱物性測定装置TPA-501を用いて23℃における室温湿気増粘型熱伝導性シリコーングリース組成物の増粘前の熱伝導率を測定した。
23±2℃/50±5%RH環境下で0.5mLの室温湿気増粘型熱伝導性シリコーングリース組成物をアルミニウム板へ円状(直径約1cm)に塗布した。塗布完了直後にアルミニウム板ごと垂直置きにし、室温湿気増粘型熱伝導性シリコーングリース組成物の移動距離(mm)を測定し、形状維持性の目安とした。即ち移動距離が少ない程形状維持性は高いことになる。
Claims (6)
- (A)25℃における粘度が0.1~1,000Pa・sであり、両末端が水酸基で封鎖されたオルガノポリシロキサン: 5~80質量部、
(B)下記一般式(1)
で表されるオルガノポリシロキサン: 20~95質量部、
(但し、(A)成分と(B)成分の合計は、100質量部である。)
(C)ケイ素原子に結合した加水分解可能な基を1分子中に3個以上有するシラン化合物及び/又はその(部分)加水分解物もしくは(部分)加水分解縮合物: 1~30質量部、
(D)増粘触媒: 0.01~20質量部、
(E)10W/m・℃以上の熱伝導率を有する熱伝導性充填剤: 100~2,000質量部、
(F)シリカ微粉末: (A)成分100質量部に対して10~100質量部
を必須成分とすることを特徴とする室温湿気増粘型熱伝導性シリコーングリース組成物。 - 更に、(G)下記一般式(2)で示されるオルガノシラン及び/又はその部分加水分解縮合物を、(A)、(B)成分の合計100質量部に対し0.1~20質量部含む請求項1記載の室温湿気増粘型熱伝導性シリコーングリース組成物。
R3 bR4 cSi(OR5)4-b-c (2)
(式中、R3は独立に炭素数6~20の非置換又は置換のアルキル基であり、R4は独立に炭素数1~20の非置換又は置換の1価炭化水素基であり、R5は独立に炭素数1~6のアルキル基であり、bは1~3の整数、cは0~2の整数で、b+cは1~3の整数である。) - 更に、(H)下記平均組成式(3)で示される25℃における粘度が0.05~1,000Pa・sのオルガノポリシロキサンを、(A)、(B)成分の合計100質量部に対し10~1,000質量部含む請求項1又は2記載の室温湿気増粘型熱伝導性シリコーングリース組成物。
R6 dSiO(4-d)/2 (3)
(式中、R6は独立に炭素数1~18の非置換又は置換の1価炭化水素基であり、dは1.8≦d≦2.2の正数である。) - 更に、(I)炭素原子を介してケイ素原子に結合したアミノ基、エポキシ基、メルカプト基、アクリロイル基及びメタクリロイル基からなる群から選択される基を有し、且つケイ素原子に結合した加水分解性基を有するシラン化合物及び/又はその部分加水分解縮合物を、(A)、(B)成分の合計100質量部に対し0.01~30質量部含む請求項1、2又は3記載の室温湿気増粘型熱伝導性シリコーングリース組成物。
- (F)成分のシリカ微粉末が、表面処理煙霧質シリカである請求項1~4のいずれか1項記載の室温湿気増粘型熱伝導性シリコーングリース組成物。
- (D)成分の増粘触媒が、グアニジル基を含有するシラン又はシロキサンである請求項1~5のいずれか1項記載の室温湿気増粘型熱伝導性シリコーングリース組成物。
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201280024854.2A CN103562318B (zh) | 2011-07-29 | 2012-05-17 | 室温湿气增粘型导热性硅脂组合物 |
RU2014107697/05A RU2014107697A (ru) | 2011-07-29 | 2012-05-17 | Композиция теплопроводящей силиконовой пластичной смазки, загущающейся при комнатной температуре и влажности |
US14/123,882 US9238734B2 (en) | 2011-07-29 | 2012-05-17 | Room temperature and humidity thickening thermo-conductive silicon grease composition |
KR1020137035111A KR101733692B1 (ko) | 2011-07-29 | 2012-05-17 | 실온 습기 증점형 열전도성 실리콘 그리스 조성물 |
EP12820265.2A EP2743315A4 (en) | 2011-07-29 | 2012-05-17 | THERMAL SILICON LUBRICANT COMPOSITION WITH THICKENING IN ROOM TEMPERATURE AND HUMIDITY |
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CN (1) | CN103562318B (ja) |
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Cited By (5)
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JP2012077256A (ja) * | 2010-10-06 | 2012-04-19 | Shin-Etsu Chemical Co Ltd | 室温湿気増粘型熱伝導性シリコーングリース組成物 |
JP2016125004A (ja) * | 2015-01-06 | 2016-07-11 | 信越化学工業株式会社 | 室温湿気硬化型熱伝導性シリコーングリース組成物 |
US20170283677A1 (en) * | 2014-09-25 | 2017-10-05 | Shin-Etsu Chemical Co., Ltd. | Uv-thickening thermally conductive silicone grease composition |
JPWO2021059936A1 (ja) * | 2019-09-27 | 2021-04-01 | ||
WO2021235259A1 (ja) * | 2020-05-22 | 2021-11-25 | 信越化学工業株式会社 | 熱伝導性シリコーン組成物、その製造方法及び半導体装置 |
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JP2014105283A (ja) * | 2012-11-28 | 2014-06-09 | Shin Etsu Chem Co Ltd | 熱伝導性シリコーングリース組成物 |
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JP6536493B2 (ja) * | 2016-06-10 | 2019-07-03 | 信越化学工業株式会社 | 耐湿性に優れた縮合硬化型シリコーン組成物の製造方法 |
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- 2012-05-17 KR KR1020137035111A patent/KR101733692B1/ko not_active Application Discontinuation
- 2012-05-17 US US14/123,882 patent/US9238734B2/en active Active
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Cited By (11)
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JP2012077256A (ja) * | 2010-10-06 | 2012-04-19 | Shin-Etsu Chemical Co Ltd | 室温湿気増粘型熱伝導性シリコーングリース組成物 |
US20170283677A1 (en) * | 2014-09-25 | 2017-10-05 | Shin-Etsu Chemical Co., Ltd. | Uv-thickening thermally conductive silicone grease composition |
JP2016125004A (ja) * | 2015-01-06 | 2016-07-11 | 信越化学工業株式会社 | 室温湿気硬化型熱伝導性シリコーングリース組成物 |
JPWO2021059936A1 (ja) * | 2019-09-27 | 2021-04-01 | ||
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CN114423825A (zh) * | 2019-09-27 | 2022-04-29 | 信越化学工业株式会社 | 导热性有机硅组合物及其制造方法、以及半导体装置 |
JP7283555B2 (ja) | 2019-09-27 | 2023-05-30 | 信越化学工業株式会社 | 熱伝導性シリコーン組成物及びその製造方法、並びに半導体装置、半導体装置の熱伝導性充填剤層の耐ポンプアウト性を改善する方法 |
CN114423825B (zh) * | 2019-09-27 | 2023-10-03 | 信越化学工业株式会社 | 导热性有机硅组合物及其制造方法、以及半导体装置 |
WO2021235259A1 (ja) * | 2020-05-22 | 2021-11-25 | 信越化学工業株式会社 | 熱伝導性シリコーン組成物、その製造方法及び半導体装置 |
JPWO2021235259A1 (ja) * | 2020-05-22 | 2021-11-25 | ||
JP7388550B2 (ja) | 2020-05-22 | 2023-11-29 | 信越化学工業株式会社 | 熱伝導性シリコーン組成物、その製造方法及び半導体装置 |
Also Published As
Publication number | Publication date |
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TWI527858B (zh) | 2016-04-01 |
EP2743315A4 (en) | 2015-02-11 |
US9238734B2 (en) | 2016-01-19 |
KR20140056191A (ko) | 2014-05-09 |
TW201315774A (zh) | 2013-04-16 |
JP2013028742A (ja) | 2013-02-07 |
RU2014107697A (ru) | 2015-09-10 |
JP5733087B2 (ja) | 2015-06-10 |
US20140094554A1 (en) | 2014-04-03 |
KR101733692B1 (ko) | 2017-05-10 |
CN103562318B (zh) | 2016-01-06 |
CN103562318A (zh) | 2014-02-05 |
EP2743315A1 (en) | 2014-06-18 |
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